{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-29",
    "results": {
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  "results": [
    {
      "spl_product_data_elements": [
        "Summit E2 Benzalkonium Chloride LAURAMINE OXIDE WATER CITRIC ACID MONOHYDRATE BENZALKONIUM CHLORIDE BENZALKONIUM PEG-120 METHYL GLUCOSE DIOLEATE GLYCERIN PHENOXYETHANOL water white - colorless, dispensed as a white foam"
      ],
      "active_ingredient": [
        "Active Ingredient Benzalkonium Chloride 0.1%"
      ],
      "purpose": [
        "Purpose Skin Antimicrobial"
      ],
      "indications_and_usage": [
        "Uses Reduces amount of bacteria on hands Recommended for repeated use"
      ],
      "warnings": [
        "Warnings For external use only. When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away."
      ],
      "keep_out_of_reach_of_children": [
        "Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away."
      ],
      "dosage_and_administration": [
        "Directions Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for at least 15 seconds. Rinse with potable water."
      ],
      "inactive_ingredient": [
        "Inactive Ingredients Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Citric Acid"
      ],
      "package_label_principal_display_panel": [
        "Package Label - 850 mL Cartridge (Front) Package Label - 850 mL Cartridge (Back)"
      ],
      "set_id": "dec25905-5b08-4866-a2a5-4c60409761fc",
      "id": "4d66824a-b004-e0c5-e063-6394a90a82f5",
      "effective_time": "20260319",
      "version": "5",
      "openfda": {
        "application_number": [
          "505G(a)(3)"
        ],
        "brand_name": [
          "Summit E2"
        ],
        "generic_name": [
          "BENZALKONIUM CHLORIDE"
        ],
        "manufacturer_name": [
          "R.L. Williams Company"
        ],
        "product_ndc": [
          "23590-300"
        ],
        "product_type": [
          "HUMAN OTC DRUG"
        ],
        "route": [
          "TOPICAL"
        ],
        "substance_name": [
          "BENZALKONIUM CHLORIDE"
        ],
        "rxcui": [
          "1233282"
        ],
        "spl_id": [
          "4d66824a-b004-e0c5-e063-6394a90a82f5"
        ],
        "spl_set_id": [
          "dec25905-5b08-4866-a2a5-4c60409761fc"
        ],
        "package_ndc": [
          "23590-300-10"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "F5UM2KM3W7"
        ]
      }
    }
  ]
}